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Brain Magnetic Resonance Imaging at 3.0 Tesla in neurodegenerative parkinsonism – a pilot study

Recruiting
Conditions
G20
G23.1
G90.3
Parkinson disease
Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]
Registration Number
DRKS00003299
Lead Sponsor
Medizinische Universität Innsbruck,Department für Neurologie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

patients:
1. clinical diagnosis of PD, MSA or PSP obtained by a neurologist according to published clinical diagnostic criteria;
2. the patient has the ability to communicate well with the investigator and comply with the requirements of the study;
3. written informed consent is obtained;

healthy controls:
1. the subject has the ability to communicate well with the investigator and comply with the requirements of the study;
2. written informed consent is obtained;

Exclusion Criteria

patients:
1. History of other neurological or psychiatric disorders or conditions;
2. the subject has a history of alcohol, narcotic, or any other drug abuse as defined by the Diagnostic and Statistical Manual of the American Psychiatric Association, 4th Edition (DSM-IV);
3. the subject is pregnant;
4. the subject is unsuitable for an MRI study (e.g. Pacemakers);

healthy controls:
1. History of neurological or psychiatric disorders or conditions;
2. the subject has a history of alcohol, narcotic, or any other drug abuse as defined by the Diagnostic and Statistical Manual of the American Psychiatric Association, 4th Edition (DSM-IV);
3. the subject is pregnant;
4. the subject is unsuitable for an MRI study

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the diagnostic value of structural MR findings using routine MRI sequences (T2, T1) at 3.0T versus 1.5T to detect atrophy or signal changes in basal ganglia and infratentorial structures for differential diagnosis of neurodegenerative parkinsonism.
Secondary Outcome Measures
NameTimeMethod
1. To identify structural changes (atrophy, signal changes) in regional brain structures that distinguish APD from PD and healthy controls and that distinguish between the different APDs; 2. To identify DWI/DTI changes in regional brain structures that distinguish PD from healthy controls; 3. To identify DWI/DTI changes in regional brain structures that distinguish APD from PD and healthy controls and that distinguish between the different APDs; 4. To identify grey or white matter changes in regional brain structures using VBM that distinguish APD from patients with PD and healthy controls as well as between the different APDs.
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